CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:The correlation factors and prognostic significance of coagulation disorders after chimeric antigen receptor T cell therapy in hematological malignancies: a cohort study.
The correlation factors and prognostic significance of coagulation disorders after chimeric antigen receptor T cell therapy in hematological malignancies: a cohort study.
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肝脏和内皮细胞的保护可能减少 CAR-T 相关凝血障碍。此外,CAR-T 细胞输注后 1 个月内发生的凝血障碍可作为血液系统恶性肿瘤患者预后的新预测指标。
除细胞因子释放综合征(CRS)和神经毒性外,凝血功能障碍是嵌合抗原受体(CAR)-T细胞治疗常见的早期并发症。然而,CAR-T 相关凝血功能障碍的机制及预后意义尚未完全明确。本研究探讨了复发/难治性血液系统恶性肿瘤患者CAR-T 细胞输注后凝血功能障碍的可能相关因素及预后意义。
本队列研究纳入2017年4月至2022年2月期间接受CAR-T 细胞治疗的56例复发/难治性血液系统恶性肿瘤患者。中位随访时间为26.8个月。凝血功能障碍定义为至少一项凝血参数异常,包括凝血酶原时间(PT)、活化部分凝血活酶时间(APTT)、凝血酶时间(TT)、纤维蛋白原和D-二聚体。采用Wilcoxon秩和检验、Fisher精确检验、配对t检验和Spearman相关系数分析凝血功能障碍的相关因素。采用Kaplan-Meier法和逐步多因素Cox回归模型分析凝血功能障碍的预后意义。
凝血功能障碍在CAR-T 细胞输注后1个月内的发生率为59%。PT延长、APTT延长、TT延长和D-二聚体升高在中位6-9天达到峰值,纤维蛋白原在中位12天降至最低值。重度CRS患者的凝血功能障碍更为显著(P<0.001)。凝血参数异常与细胞因子、CAR-T 细胞、肝功能参数及血管性血友病因子(VWF)在峰值水平和峰值时间上均密切相关(P<0.05)。统计分析显示,凝血功能障碍与CAR-T 治疗中更高的初始缓解率相关(TT,P=0.006;D-二聚体,P=0.010),同时也与更长的无进展生存期(PFS)相关(PT,P=0.017;APTT,P=0.018;TT,P=0.001;纤维蛋白原,P=0.003;D-二聚体,P<0.001),其中TT延长(HR=0.279,95% CI:0.099-0.782,P=0.015)和D-二聚体升高(HR=0.218,95% CI:0.087-0.548,P=0.001)是PFS的独立预测因素。
Along with cytokine release syndrome (CRS) and neurotoxicity, coagulation disorder is a common early complication of chimeric antigen receptor (CAR)-T cell therapy. However, the mechanisms and prognostic significance of CAR-T-related coagulation disorders are not fully known. This study explored the possible correlation factors and prognostic significance of coagulation disorders after CAR-T cell infusion in patients with relapsed/refractory hematological malignancies.
This cohort study included 56 patients with relapsed/refractory hematological malignancies who were treated with CAR-T cells between April 2017 and February 2022. The median follow-up was 26.8 months. Coagulation disorders were defined as the abnormality in at least one coagulation parameters, including prothrombin time (PT), activated partial thromboplastin time (APTT), thrombin time (TT), fibrinogen, and D-dimer. The correlation factors of coagulation disorders were analyzed using Wilcoxon rank-sum test, Fisher's exact test, paired t -test and Spearman correlation coefficient. The prognostic significance of coagulation disorders was analyzed using Kaplan-Meier method and stepwise multivariate Cox regression model.
The incidence of coagulation disorders was 59% within 1 month of CAR-T cell infusion. PT prolongation, APTT prolongation, TT prolongation, and D-dimer increase peaked at a median of 6-9 days, and fibrinogen decreased to its lowest value at a median of 12 days. Coagulation disorders in patients with severe CRS were more significant (P<0.001). Abnormality of coagulation parameters was closely related to cytokines, CAR-T cells, liver function parameters, and von Willebrand Factor (VWF) in both peak level and peak time (P<0.05). Statistical analysis showed that coagulation disorders were associated with higher initial response rates (TT, P=0.006; D-dimer, P=0.010) and also longer progression-free survival (PFS) (PT, P=0.017; APTT, P=0.018; TT, P=0.001; Fibrinogen, P=0.003; D-dimer, P<0.001) in CAR-T therapy, with TT prolongation (HR =0.279, 95% CI: 0.099-0.782, P=0.015) and D-dimer increase (HR =0.218, 95% CI: 0.087-0.548, P=0.001) independent predictors for PFS.
The protection of liver and endothelial cells may reduce CAR-T-related coagulation disorders. Further, coagulation disorders occurring within 1 month of CAR-T cell infusion can serve as a new predictor for prognosis in patients with hematological malignancies.
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